Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
9 | g.36245961_36246193delinsCTA | CA2573144542 | CLTA,GNE | c.547_709+70delinsTAG c.277_439+70delinsTAG c.454_616+70delinsTAG c.486-17237_486-17005delinsCTA (n.486-17237_486-17005delinsCTA) c.439_601+70delinsTAG | ClinVar dbSNP |
9 | g.36246131A>C | CA373418340 | CLTA,GNE | c.609T>G (p.Cys203Trp) c.339T>G (p.Cys113Trp) c.516T>G (p.Cys172Trp) c.486-17067A>C (n.486-17067A>C) c.501T>G (p.Cys167Trp) | |
9 | g.36246131A>G | CA464619812 | CLTA,GNE | c.609T>C (p.Cys203=) c.339T>C (p.Cys113=) c.516T>C (p.Cys172=) c.486-17067A>G (n.486-17067A>G) c.501T>C (p.Cys167=) | |
9 | g.36246131A>T | CA373418342 | CLTA,GNE | c.609T>A (p.Cys203Ter) c.339T>A (p.Cys113Ter) c.516T>A (p.Cys172Ter) c.486-17067A>T (n.486-17067A>T) c.501T>A (p.Cys167Ter) | |
9 | g.36246132C>A | CA373418343 | CLTA,GNE | c.608G>T (p.Cys203Phe) c.338G>T (p.Cys113Phe) c.515G>T (p.Cys172Phe) c.486-17066C>A (n.486-17066C>A) c.500G>T (p.Cys167Phe) | |
9 | g.36246132C= | CA1846375251 | CLTA,GNE | c.608G= (p.Cys203=) c.338G= (p.Cys113=) c.515G= (p.Cys172=) c.486-17066C= (n.486-17066C=) c.500G= (p.Cys167=) | |
9 | g.36246132C>G | CA5056718 | CLTA,GNE | c.608G>C (p.Cys203Ser) c.338G>C (p.Cys113Ser) c.515G>C (p.Cys172Ser) c.486-17066C>G (n.486-17066C>G) c.500G>C (p.Cys167Ser) | dbSNP ExAC gnomAD v2 gnomAD v4 |
9 | g.36246132C>T | CA373418346 | CLTA,GNE | c.608G>A (p.Cys203Tyr) c.338G>A (p.Cys113Tyr) c.515G>A (p.Cys172Tyr) c.486-17066C>T (n.486-17066C>T) c.500G>A (p.Cys167Tyr) | dbSNP gnomAD v3 gnomAD v4 |
9 | g.36246133A>C | CA373418350 | CLTA,GNE | c.607T>G (p.Cys203Gly) c.337T>G (p.Cys113Gly) c.514T>G (p.Cys172Gly) c.486-17065A>C (n.486-17065A>C) c.499T>G (p.Cys167Gly) | |
9 | g.36246133A>G | CA373418349 | CLTA,GNE | c.607T>C (p.Cys203Arg) c.337T>C (p.Cys113Arg) c.514T>C (p.Cys172Arg) c.486-17065A>G (n.486-17065A>G) c.499T>C (p.Cys167Arg) | |
9 | g.36246133A>T | CA373418348 | CLTA,GNE | c.607T>A (p.Cys203Ser) c.337T>A (p.Cys113Ser) c.514T>A (p.Cys172Ser) c.486-17065A>T (n.486-17065A>T) c.499T>A (p.Cys167Ser) | |
9 | g.36246134C>A | CA373418352 | CLTA,GNE | c.606G>T (p.Met202Ile) c.336G>T (p.Met112Ile) c.513G>T (p.Met171Ile) c.486-17064C>A (n.486-17064C>A) c.498G>T (p.Met166Ile) | |
9 | g.36246134C>G | CA373418353 | CLTA,GNE | c.606G>C (p.Met202Ile) c.336G>C (p.Met112Ile) c.513G>C (p.Met171Ile) c.486-17064C>G (n.486-17064C>G) c.498G>C (p.Met166Ile) | |
9 | g.36246134C>T | CA373418355 | CLTA,GNE | c.606G>A (p.Met202Ile) c.336G>A (p.Met112Ile) c.513G>A (p.Met171Ile) c.486-17064C>T (n.486-17064C>T) c.498G>A (p.Met166Ile) | |
9 | g.36246135A>C | CA373418358 | CLTA,GNE | c.605T>G (p.Met202Arg) c.335T>G (p.Met112Arg) c.512T>G (p.Met171Arg) c.486-17063A>C (n.486-17063A>C) c.497T>G (p.Met166Arg) | |
9 | g.36246135A>G | CA373418359 | CLTA,GNE | c.605T>C (p.Met202Thr) c.335T>C (p.Met112Thr) c.512T>C (p.Met171Thr) c.486-17063A>G (n.486-17063A>G) c.497T>C (p.Met166Thr) | ClinVar |
9 | g.36246135A>T | CA373418361 | CLTA,GNE | c.605T>A (p.Met202Lys) c.335T>A (p.Met112Lys) c.512T>A (p.Met171Lys) c.486-17063A>T (n.486-17063A>T) c.497T>A (p.Met166Lys) | |
9 | g.36246136T>A | CA373418364 | CLTA,GNE | c.604A>T (p.Met202Leu) c.334A>T (p.Met112Leu) c.511A>T (p.Met171Leu) c.486-17062T>A (n.486-17062T>A) c.496A>T (p.Met166Leu) | |
9 | g.36246136T>C | CA253719 | CLTA,GNE | c.604A>G (p.Met202Val) c.334A>G (p.Met112Val) c.511A>G (p.Met171Val) c.486-17062T>C (n.486-17062T>C) c.496A>G (p.Met166Val) | ClinVar dbSNP gnomAD v4 |
9 | g.36246136T>G | CA373418365 | CLTA,GNE | c.604A>C (p.Met202Leu) c.334A>C (p.Met112Leu) c.511A>C (p.Met171Leu) c.486-17062T>G (n.486-17062T>G) c.496A>C (p.Met166Leu) | |
9 | g.36246136T= | CA1846375255 | CLTA,GNE | c.604A= (p.Met202=) c.334A= (p.Met112=) c.511A= (p.Met171=) c.486-17062T= (n.486-17062T=) c.496A= (p.Met166=) | |
9 | g.36246137G>A | CA464619824 | CLTA,GNE | c.603C>T (p.Ser201=) c.333C>T (p.Ser111=) c.510C>T (p.Ser170=) c.486-17061G>A (n.486-17061G>A) c.495C>T (p.Ser165=) | |
9 | g.36246137G>C | CA464619826 | CLTA,GNE | c.603C>G (p.Ser201=) c.333C>G (p.Ser111=) c.510C>G (p.Ser170=) c.486-17061G>C (n.486-17061G>C) c.495C>G (p.Ser165=) | |
9 | g.36246137G>T | CA464619825 | CLTA,GNE | c.603C>A (p.Ser201=) c.333C>A (p.Ser111=) c.510C>A (p.Ser170=) c.486-17061G>T (n.486-17061G>T) c.495C>A (p.Ser165=) | |
9 | g.36246138G>A | CA373418368 | CLTA,GNE | c.602C>T (p.Ser201Phe) c.332C>T (p.Ser111Phe) c.509C>T (p.Ser170Phe) c.486-17060G>A (n.486-17060G>A) c.494C>T (p.Ser165Phe) | |
9 | g.36246138G>C | CA373418370 | CLTA,GNE | c.602C>G (p.Ser201Cys) c.332C>G (p.Ser111Cys) c.509C>G (p.Ser170Cys) c.486-17060G>C (n.486-17060G>C) c.494C>G (p.Ser165Cys) | |
9 | g.36246138G>T | CA373418371 | CLTA,GNE | c.602C>A (p.Ser201Tyr) c.332C>A (p.Ser111Tyr) c.509C>A (p.Ser170Tyr) c.486-17060G>T (n.486-17060G>T) c.494C>A (p.Ser165Tyr) | |
9 | g.36246139A>C | CA373418375 | CLTA,GNE | c.601T>G (p.Ser201Ala) c.331T>G (p.Ser111Ala) c.508T>G (p.Ser170Ala) c.486-17059A>C (n.486-17059A>C) c.493T>G (p.Ser165Ala) | |
9 | g.36246139A>G | CA373418378 | CLTA,GNE | c.601T>C (p.Ser201Pro) c.331T>C (p.Ser111Pro) c.508T>C (p.Ser170Pro) c.486-17059A>G (n.486-17059A>G) c.493T>C (p.Ser165Pro) | gnomAD v4 |
9 | g.36246139A>T | CA373418376 | CLTA,GNE | c.601T>A (p.Ser201Thr) c.331T>A (p.Ser111Thr) c.508T>A (p.Ser170Thr) c.486-17059A>T (n.486-17059A>T) c.493T>A (p.Ser165Thr) | gnomAD v4 |
9 | g.36246140T>A | CA464619832 | CLTA,GNE | c.600A>T (p.Ile200=) c.330A>T (p.Ile110=) c.507A>T (p.Ile169=) c.486-17058T>A (n.486-17058T>A) c.492A>T (p.Ile164=) | |
9 | g.36246140T>C | CA373418380 | CLTA,GNE | c.600A>G (p.Ile200Met) c.330A>G (p.Ile110Met) c.507A>G (p.Ile169Met) c.486-17058T>C (n.486-17058T>C) c.492A>G (p.Ile164Met) | |
9 | g.36246140T>G | CA464619837 | CLTA,GNE | c.600A>C (p.Ile200=) c.330A>C (p.Ile110=) c.507A>C (p.Ile169=) c.486-17058T>G (n.486-17058T>G) c.492A>C (p.Ile164=) | |
9 | g.36246141A>C | CA373418385 | CLTA,GNE | c.599T>G (p.Ile200Arg) c.329T>G (p.Ile110Arg) c.506T>G (p.Ile169Arg) c.486-17057A>C (n.486-17057A>C) c.491T>G (p.Ile164Arg) | |
9 | g.36246141A>G | CA373418382 | CLTA,GNE | c.599T>C (p.Ile200Thr) c.329T>C (p.Ile110Thr) c.506T>C (p.Ile169Thr) c.486-17057A>G (n.486-17057A>G) c.491T>C (p.Ile164Thr) | |
9 | g.36246141A>T | CA373418387 | CLTA,GNE | c.599T>A (p.Ile200Lys) c.329T>A (p.Ile110Lys) c.506T>A (p.Ile169Lys) c.486-17057A>T (n.486-17057A>T) c.491T>A (p.Ile164Lys) | |
9 | g.36246142T>A | CA373418390 | CLTA,GNE | c.598A>T (p.Ile200Leu) c.328A>T (p.Ile110Leu) c.505A>T (p.Ile169Leu) c.486-17056T>A (n.486-17056T>A) c.490A>T (p.Ile164Leu) | |
9 | g.36246142T>C | CA373418391 | CLTA,GNE | c.598A>G (p.Ile200Val) c.328A>G (p.Ile110Val) c.505A>G (p.Ile169Val) c.486-17056T>C (n.486-17056T>C) c.490A>G (p.Ile164Val) | |
9 | g.36246142T>G | CA373418393 | CLTA,GNE | c.598A>C (p.Ile200Leu) c.328A>C (p.Ile110Leu) c.505A>C (p.Ile169Leu) c.486-17056T>G (n.486-17056T>G) c.490A>C (p.Ile164Leu) | |
9 | g.36246143C>A | CA464619844 | CLTA,GNE | c.597G>T (p.Leu199=) c.327G>T (p.Leu109=) c.504G>T (p.Leu168=) c.486-17055C>A (n.486-17055C>A) c.489G>T (p.Leu163=) | |
9 | g.36246143C>G | CA464619845 | CLTA,GNE | c.597G>C (p.Leu199=) c.327G>C (p.Leu109=) c.504G>C (p.Leu168=) c.486-17055C>G (n.486-17055C>G) c.489G>C (p.Leu163=) | |
9 | g.36246143C>T | CA464619846 | CLTA,GNE | c.597G>A (p.Leu199=) c.327G>A (p.Leu109=) c.504G>A (p.Leu168=) c.486-17055C>T (n.486-17055C>T) c.489G>A (p.Leu163=) | |
9 | g.36246144A>C | CA373418395 | CLTA,GNE | c.596T>G (p.Leu199Arg) c.326T>G (p.Leu109Arg) c.503T>G (p.Leu168Arg) c.486-17054A>C (n.486-17054A>C) c.488T>G (p.Leu163Arg) | |
9 | g.36246144A>G | CA373418396 | CLTA,GNE | c.596T>C (p.Leu199Pro) c.326T>C (p.Leu109Pro) c.503T>C (p.Leu168Pro) c.486-17054A>G (n.486-17054A>G) c.488T>C (p.Leu163Pro) | ClinVar |
9 | g.36246144A>T | CA373418397 | CLTA,GNE | c.596T>A (p.Leu199Gln) c.326T>A (p.Leu109Gln) c.503T>A (p.Leu168Gln) c.486-17054A>T (n.486-17054A>T) c.488T>A (p.Leu163Gln) | |
9 | g.36246145G>A | CA464619852 | CLTA,GNE | c.595C>T (p.Leu199=) c.325C>T (p.Leu109=) c.502C>T (p.Leu168=) c.486-17053G>A (n.486-17053G>A) c.487C>T (p.Leu163=) | gnomAD v4 |
9 | g.36246145G>C | CA373418399 | CLTA,GNE | c.595C>G (p.Leu199Val) c.325C>G (p.Leu109Val) c.502C>G (p.Leu168Val) c.486-17053G>C (n.486-17053G>C) c.487C>G (p.Leu163Val) | |
9 | g.36246145G>T | CA373418401 | CLTA,GNE | c.595C>A (p.Leu199Met) c.325C>A (p.Leu109Met) c.502C>A (p.Leu168Met) c.486-17053G>T (n.486-17053G>T) c.487C>A (p.Leu163Met) | |
9 | g.36246146G>A | CA464619856 | CLTA,GNE | c.594C>T (p.His198=) c.324C>T (p.His108=) c.501C>T (p.His167=) c.486-17052G>A (n.486-17052G>A) c.486C>T (p.His162=) | ClinVar dbSNP gnomAD v4 |
9 | g.36246146G>C | CA373418403 | CLTA,GNE | c.594C>G (p.His198Gln) c.324C>G (p.His108Gln) c.501C>G (p.His167Gln) c.486-17052G>C (n.486-17052G>C) c.486C>G (p.His162Gln) | |
9 | g.36246146G= | CA1846375263 | CLTA,GNE | c.594C= (p.His198=) c.324C= (p.His108=) c.501C= (p.His167=) c.486-17052G= (n.486-17052G=) c.486C= (p.His162=) | |
9 | g.36246146G>T | CA373418404 | CLTA,GNE | c.594C>A (p.His198Gln) c.324C>A (p.His108Gln) c.501C>A (p.His167Gln) c.486-17052G>T (n.486-17052G>T) c.486C>A (p.His162Gln) | ClinVar dbSNP |
9 | g.36246147T>A | CA373418405 | CLTA,GNE | c.593A>T (p.His198Leu) c.323A>T (p.His108Leu) c.500A>T (p.His167Leu) c.486-17051T>A (n.486-17051T>A) c.485A>T (p.His162Leu) | |
9 | g.36246147T>C | CA373418406 | CLTA,GNE | c.593A>G (p.His198Arg) c.323A>G (p.His108Arg) c.500A>G (p.His167Arg) c.486-17051T>C (n.486-17051T>C) c.485A>G (p.His162Arg) | |
9 | g.36246147T>G | CA373418407 | CLTA,GNE | c.593A>C (p.His198Pro) c.323A>C (p.His108Pro) c.500A>C (p.His167Pro) c.486-17051T>G (n.486-17051T>G) c.485A>C (p.His162Pro) | |
9 | g.36246148G>A | CA373418410 | CLTA,GNE | c.592C>T (p.His198Tyr) c.322C>T (p.His108Tyr) c.499C>T (p.His167Tyr) c.486-17050G>A (n.486-17050G>A) c.484C>T (p.His162Tyr) | |
9 | g.36246148G>C | CA373418413 | CLTA,GNE | c.592C>G (p.His198Asp) c.322C>G (p.His108Asp) c.499C>G (p.His167Asp) c.486-17050G>C (n.486-17050G>C) c.484C>G (p.His162Asp) | |
9 | g.36246148G>T | CA373418412 | CLTA,GNE | c.592C>A (p.His198Asn) c.322C>A (p.His108Asn) c.499C>A (p.His167Asn) c.486-17050G>T (n.486-17050G>T) c.484C>A (p.His162Asn) | |
9 | g.36246149C>A | CA373418416 | CLTA,GNE | c.591G>T (p.Gln197His) c.321G>T (p.Gln107His) c.498G>T (p.Gln166His) c.486-17049C>A (n.486-17049C>A) c.483G>T (p.Gln161His) | |
9 | g.36246149C= | CA1846375273 | CLTA,GNE | c.591G= (p.Gln197=) c.321G= (p.Gln107=) c.498G= (p.Gln166=) c.486-17049C= (n.486-17049C=) c.483G= (p.Gln161=) | |
9 | g.36246149C>G | CA373418418 | CLTA,GNE | c.591G>C (p.Gln197His) c.321G>C (p.Gln107His) c.498G>C (p.Gln166His) c.486-17049C>G (n.486-17049C>G) c.483G>C (p.Gln161His) | ClinVar dbSNP gnomAD v4 |
9 | g.36246149C>T | CA464619860 | CLTA,GNE | c.591G>A (p.Gln197=) c.321G>A (p.Gln107=) c.498G>A (p.Gln166=) c.486-17049C>T (n.486-17049C>T) c.483G>A (p.Gln161=) | |
9 | g.36246150T>A | CA373418420 | CLTA,GNE | c.590A>T (p.Gln197Leu) c.320A>T (p.Gln107Leu) c.497A>T (p.Gln166Leu) c.486-17048T>A (n.486-17048T>A) c.482A>T (p.Gln161Leu) | |
9 | g.36246150T>C | CA373418422 | CLTA,GNE | c.590A>G (p.Gln197Arg) c.320A>G (p.Gln107Arg) c.497A>G (p.Gln166Arg) c.486-17048T>C (n.486-17048T>C) c.482A>G (p.Gln161Arg) | |
9 | g.36246150T>G | CA373418424 | CLTA,GNE | c.590A>C (p.Gln197Pro) c.320A>C (p.Gln107Pro) c.497A>C (p.Gln166Pro) c.486-17048T>G (n.486-17048T>G) c.482A>C (p.Gln161Pro) | |
9 | g.36246151G>A | CA373418427 | CLTA,GNE | c.589C>T (p.Gln197Ter) c.319C>T (p.Gln107Ter) c.496C>T (p.Gln166Ter) c.486-17047G>A (n.486-17047G>A) c.481C>T (p.Gln161Ter) | |
9 | g.36246151G>C | CA373418428 | CLTA,GNE | c.589C>G (p.Gln197Glu) c.319C>G (p.Gln107Glu) c.496C>G (p.Gln166Glu) c.486-17047G>C (n.486-17047G>C) c.481C>G (p.Gln161Glu) | |
9 | g.36246151G>T | CA373418430 | CLTA,GNE | c.589C>A (p.Gln197Lys) c.319C>A (p.Gln107Lys) c.496C>A (p.Gln166Lys) c.486-17047G>T (n.486-17047G>T) c.481C>A (p.Gln161Lys) | |
9 | g.36246152C>A | CA373418432 | CLTA,GNE | c.588G>T (p.Glu196Asp) c.318G>T (p.Glu106Asp) c.495G>T (p.Glu165Asp) c.486-17046C>A (n.486-17046C>A) c.480G>T (p.Glu160Asp) | |
9 | g.36246152C>G | CA373418434 | CLTA,GNE | c.588G>C (p.Glu196Asp) c.318G>C (p.Glu106Asp) c.495G>C (p.Glu165Asp) c.486-17046C>G (n.486-17046C>G) c.480G>C (p.Glu160Asp) | |
9 | g.36246152C>T | CA464619867 | CLTA,GNE | c.588G>A (p.Glu196=) c.318G>A (p.Glu106=) c.495G>A (p.Glu165=) c.486-17046C>T (n.486-17046C>T) c.480G>A (p.Glu160=) | ClinVar dbSNP gnomAD v4 |
9 | g.36246153T>A | CA373418440 | CLTA,GNE | c.587A>T (p.Glu196Val) c.317A>T (p.Glu106Val) c.494A>T (p.Glu165Val) c.486-17045T>A (n.486-17045T>A) c.479A>T (p.Glu160Val) | |
9 | g.36246153T>C | CA373418438 | CLTA,GNE | c.587A>G (p.Glu196Gly) c.317A>G (p.Glu106Gly) c.494A>G (p.Glu165Gly) c.486-17045T>C (n.486-17045T>C) c.479A>G (p.Glu160Gly) | |
9 | g.36246153T>G | CA373418436 | CLTA,GNE | c.587A>C (p.Glu196Ala) c.317A>C (p.Glu106Ala) c.494A>C (p.Glu165Ala) c.486-17045T>G (n.486-17045T>G) c.479A>C (p.Glu160Ala) | |
9 | g.36246154C>A | CA373418442 | CLTA,GNE | c.586G>T (p.Glu196Ter) c.316G>T (p.Glu106Ter) c.493G>T (p.Glu165Ter) c.486-17044C>A (n.486-17044C>A) c.478G>T (p.Glu160Ter) | |
9 | g.36246154C>G | CA373418443 | CLTA,GNE | c.586G>C (p.Glu196Gln) c.316G>C (p.Glu106Gln) c.493G>C (p.Glu165Gln) c.486-17044C>G (n.486-17044C>G) c.478G>C (p.Glu160Gln) | |
9 | g.36246154C>T | CA373418445 | CLTA,GNE | c.586G>A (p.Glu196Lys) c.316G>A (p.Glu106Lys) c.493G>A (p.Glu165Lys) c.486-17044C>T (n.486-17044C>T) c.478G>A (p.Glu160Lys) | |
9 | g.36246155T>A | CA464619875 | CLTA,GNE | c.585A>T (p.Ala195=) c.315A>T (p.Ala105=) c.492A>T (p.Ala164=) c.486-17043T>A (n.486-17043T>A) c.477A>T (p.Ala159=) | |
9 | g.36246155T>C | CA464619878 | CLTA,GNE | c.585A>G (p.Ala195=) c.315A>G (p.Ala105=) c.492A>G (p.Ala164=) c.486-17043T>C (n.486-17043T>C) c.477A>G (p.Ala159=) | |
9 | g.36246155T>G | CA464619877 | CLTA,GNE | c.585A>C (p.Ala195=) c.315A>C (p.Ala105=) c.492A>C (p.Ala164=) c.486-17043T>G (n.486-17043T>G) c.477A>C (p.Ala159=) | |
9 | g.36246156G>A | CA373418448 | CLTA,GNE | c.584C>T (p.Ala195Val) c.314C>T (p.Ala105Val) c.491C>T (p.Ala164Val) c.486-17042G>A (n.486-17042G>A) c.476C>T (p.Ala159Val) | dbSNP gnomAD v2 gnomAD v4 |
9 | g.36246156G>C | CA373418450 | CLTA,GNE | c.584C>G (p.Ala195Gly) c.314C>G (p.Ala105Gly) c.491C>G (p.Ala164Gly) c.486-17042G>C (n.486-17042G>C) c.476C>G (p.Ala159Gly) | |
9 | g.36246156G= | CA1846375276 | CLTA,GNE | c.584C= (p.Ala195=) c.314C= (p.Ala105=) c.491C= (p.Ala164=) c.486-17042G= (n.486-17042G=) c.476C= (p.Ala159=) | |
9 | g.36246156G>T | CA373418451 | CLTA,GNE | c.584C>A (p.Ala195Glu) c.314C>A (p.Ala105Glu) c.491C>A (p.Ala164Glu) c.486-17042G>T (n.486-17042G>T) c.476C>A (p.Ala159Glu) | |
9 | g.36246157C>A | CA373418454 | CLTA,GNE | c.583G>T (p.Ala195Ser) c.313G>T (p.Ala105Ser) c.490G>T (p.Ala164Ser) c.486-17041C>A (n.486-17041C>A) c.475G>T (p.Ala159Ser) | |
9 | g.36246157C>G | CA373418456 | CLTA,GNE | c.583G>C (p.Ala195Pro) c.313G>C (p.Ala105Pro) c.490G>C (p.Ala164Pro) c.486-17041C>G (n.486-17041C>G) c.475G>C (p.Ala159Pro) | |
9 | g.36246157C>T | CA373418458 | CLTA,GNE | c.583G>A (p.Ala195Thr) c.313G>A (p.Ala105Thr) c.490G>A (p.Ala164Thr) c.486-17041C>T (n.486-17041C>T) c.475G>A (p.Ala159Thr) | ClinVar COSMIC COSMIC COSMIC |
9 | g.36246158A= | CA1846375280 | CLTA,GNE | c.582T= (p.Ser194=) c.312T= (p.Ser104=) c.489T= (p.Ser163=) c.486-17040A= (n.486-17040A=) c.474T= (p.Ser158=) | |
9 | g.36246158A>C | CA373418460 | CLTA,GNE | c.582T>G (p.Ser194Arg) c.312T>G (p.Ser104Arg) c.489T>G (p.Ser163Arg) c.486-17040A>C (n.486-17040A>C) c.474T>G (p.Ser158Arg) | |
9 | g.36246158A>G | CA5056719 | CLTA,GNE | c.582T>C (p.Ser194=) c.312T>C (p.Ser104=) c.489T>C (p.Ser163=) c.486-17040A>G (n.486-17040A>G) c.474T>C (p.Ser158=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
9 | g.36246158A>T | CA373418463 | CLTA,GNE | c.582T>A (p.Ser194Arg) c.312T>A (p.Ser104Arg) c.489T>A (p.Ser163Arg) c.486-17040A>T (n.486-17040A>T) c.474T>A (p.Ser158Arg) | |
9 | g.36246159C>A | CA373418468 | CLTA,GNE | c.581G>T (p.Ser194Ile) c.311G>T (p.Ser104Ile) c.488G>T (p.Ser163Ile) c.486-17039C>A (n.486-17039C>A) c.473G>T (p.Ser158Ile) | |
9 | g.36246159C>G | CA373418466 | CLTA,GNE | c.581G>C (p.Ser194Thr) c.311G>C (p.Ser104Thr) c.488G>C (p.Ser163Thr) c.486-17039C>G (n.486-17039C>G) c.473G>C (p.Ser158Thr) | |
9 | g.36246159C>T | CA373418464 | CLTA,GNE | c.581G>A (p.Ser194Asn) c.311G>A (p.Ser104Asn) c.488G>A (p.Ser163Asn) c.486-17039C>T (n.486-17039C>T) c.473G>A (p.Ser158Asn) | |
9 | g.36246160T>A | CA373418470 | CLTA,GNE | c.580A>T (p.Ser194Cys) c.310A>T (p.Ser104Cys) c.487A>T (p.Ser163Cys) c.486-17038T>A (n.486-17038T>A) c.472A>T (p.Ser158Cys) | |
9 | g.36246160T>C | CA5056720 | CLTA,GNE | c.580A>G (p.Ser194Gly) c.310A>G (p.Ser104Gly) c.487A>G (p.Ser163Gly) c.486-17038T>C (n.486-17038T>C) c.472A>G (p.Ser158Gly) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.36246160T>G | CA373418473 | CLTA,GNE | c.580A>C (p.Ser194Arg) c.310A>C (p.Ser104Arg) c.487A>C (p.Ser163Arg) c.486-17038T>G (n.486-17038T>G) c.472A>C (p.Ser158Arg) | |
9 | g.36246160T= | CA1846375285 | CLTA,GNE | c.580A= (p.Ser194=) c.310A= (p.Ser104=) c.487A= (p.Ser163=) c.486-17038T= (n.486-17038T=) c.472A= (p.Ser158=) | |
9 | g.36246161G>A | CA464619885 | CLTA,GNE | c.579C>T (p.Arg193=) c.309C>T (p.Arg103=) c.486C>T (p.Arg162=) c.486-17037G>A (n.486-17037G>A) c.471C>T (p.Arg157=) | dbSNP gnomAD v2 gnomAD v4 |
9 | g.36246161G>C | CA464619886 | CLTA,GNE | c.579C>G (p.Arg193=) c.309C>G (p.Arg103=) c.486C>G (p.Arg162=) c.486-17037G>C (n.486-17037G>C) c.471C>G (p.Arg157=) | |
9 | g.36246161G= | CA1846375289 | CLTA,GNE | c.579C= (p.Arg193=) c.309C= (p.Arg103=) c.486C= (p.Arg162=) c.486-17037G= (n.486-17037G=) c.471C= (p.Arg157=) | |
9 | g.36246161G>T | CA464619887 | CLTA,GNE | c.579C>A (p.Arg193=) c.309C>A (p.Arg103=) c.486C>A (p.Arg162=) c.486-17037G>T (n.486-17037G>T) c.471C>A (p.Arg157=) | |
9 | g.36246162C>A | CA373418475 | CLTA,GNE | c.578G>T (p.Arg193Leu) c.308G>T (p.Arg103Leu) c.485G>T (p.Arg162Leu) c.486-17036C>A (n.486-17036C>A) c.470G>T (p.Arg157Leu) | |
9 | g.36246162C= | CA1846375291 | CLTA,GNE | c.578G= (p.Arg193=) c.308G= (p.Arg103=) c.485G= (p.Arg162=) c.486-17036C= (n.486-17036C=) c.470G= (p.Arg157=) | |
9 | g.36246162C>G | CA373418477 | CLTA,GNE | c.578G>C (p.Arg193Pro) c.308G>C (p.Arg103Pro) c.485G>C (p.Arg162Pro) c.486-17036C>G (n.486-17036C>G) c.470G>C (p.Arg157Pro) | |
9 | g.36246162C>T | CA5056721 | CLTA,GNE | c.578G>A (p.Arg193His) c.308G>A (p.Arg103His) c.485G>A (p.Arg162His) c.486-17036C>T (n.486-17036C>T) c.470G>A (p.Arg157His) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.36246163G>A | CA5056722 | CLTA,GNE | c.577C>T (p.Arg193Cys) c.307C>T (p.Arg103Cys) c.484C>T (p.Arg162Cys) c.486-17035G>A (n.486-17035G>A) c.469C>T (p.Arg157Cys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
9 | g.36246163G>C | CA373418481 | CLTA,GNE | c.577C>G (p.Arg193Gly) c.307C>G (p.Arg103Gly) c.484C>G (p.Arg162Gly) c.486-17035G>C (n.486-17035G>C) c.469C>G (p.Arg157Gly) | dbSNP gnomAD v2 gnomAD v4 |
9 | g.36246163G= | CA1846375295 | CLTA,GNE | c.577C= (p.Arg193=) c.307C= (p.Arg103=) c.484C= (p.Arg162=) c.486-17035G= (n.486-17035G=) c.469C= (p.Arg157=) | |
9 | g.36246163G>T | CA373418484 | CLTA,GNE | c.577C>A (p.Arg193Ser) c.307C>A (p.Arg103Ser) c.484C>A (p.Arg162Ser) c.486-17035G>T (n.486-17035G>T) c.469C>A (p.Arg157Ser) | |
9 | g.36246164G>A | CA464619891 | CLTA,GNE | c.576C>T (p.Thr192=) c.306C>T (p.Thr102=) c.483C>T (p.Thr161=) c.486-17034G>A (n.486-17034G>A) c.468C>T (p.Thr156=) | dbSNP gnomAD v2 gnomAD v4 |
9 | g.36246164G>C | CA464619892 | CLTA,GNE | c.576C>G (p.Thr192=) c.306C>G (p.Thr102=) c.483C>G (p.Thr161=) c.486-17034G>C (n.486-17034G>C) c.468C>G (p.Thr156=) | |
9 | g.36246164G= | CA1846375298 | CLTA,GNE | c.576C= (p.Thr192=) c.306C= (p.Thr102=) c.483C= (p.Thr161=) c.486-17034G= (n.486-17034G=) c.468C= (p.Thr156=) | |
9 | g.36246164G>T | CA464619893 | CLTA,GNE | c.576C>A (p.Thr192=) c.306C>A (p.Thr102=) c.483C>A (p.Thr161=) c.486-17034G>T (n.486-17034G>T) c.468C>A (p.Thr156=) | |
9 | g.36246165G>A | CA373418486 | CLTA,GNE | c.575C>T (p.Thr192Ile) c.305C>T (p.Thr102Ile) c.482C>T (p.Thr161Ile) c.486-17033G>A (n.486-17033G>A) c.467C>T (p.Thr156Ile) | |
9 | g.36246165G>C | CA373418487 | CLTA,GNE | c.575C>G (p.Thr192Ser) c.305C>G (p.Thr102Ser) c.482C>G (p.Thr161Ser) c.486-17033G>C (n.486-17033G>C) c.467C>G (p.Thr156Ser) | |
9 | g.36246165G>T | CA373418489 | CLTA,GNE | c.575C>A (p.Thr192Asn) c.305C>A (p.Thr102Asn) c.482C>A (p.Thr161Asn) c.486-17033G>T (n.486-17033G>T) c.467C>A (p.Thr156Asn) | |
9 | g.36246166T>A | CA373418494 | CLTA,GNE | c.574A>T (p.Thr192Ser) c.304A>T (p.Thr102Ser) c.481A>T (p.Thr161Ser) c.486-17032T>A (n.486-17032T>A) c.466A>T (p.Thr156Ser) | |
9 | g.36246166T>C | CA373418492 | CLTA,GNE | c.574A>G (p.Thr192Ala) c.304A>G (p.Thr102Ala) c.481A>G (p.Thr161Ala) c.486-17032T>C (n.486-17032T>C) c.466A>G (p.Thr156Ala) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
9 | g.36246166T>G | CA373418491 | CLTA,GNE | c.574A>C (p.Thr192Pro) c.304A>C (p.Thr102Pro) c.481A>C (p.Thr161Pro) c.486-17032T>G (n.486-17032T>G) c.466A>C (p.Thr156Pro) | dbSNP gnomAD v2 gnomAD v4 |
9 | g.36246166T= | CA1846375305 | CLTA,GNE | c.574A= (p.Thr192=) c.304A= (p.Thr102=) c.481A= (p.Thr161=) c.486-17032T= (n.486-17032T=) c.466A= (p.Thr156=) | |
9 | g.36246167G>A | CA464619898 | CLTA,GNE | c.573C>T (p.Cys191=) c.303C>T (p.Cys101=) c.480C>T (p.Cys160=) c.486-17031G>A (n.486-17031G>A) c.465C>T (p.Cys155=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
9 | g.36246167G>C | CA373418496 | CLTA,GNE | c.573C>G (p.Cys191Trp) c.303C>G (p.Cys101Trp) c.480C>G (p.Cys160Trp) c.486-17031G>C (n.486-17031G>C) c.465C>G (p.Cys155Trp) | |
9 | g.36246167G= | CA1846375310 | CLTA,GNE | c.573C= (p.Cys191=) c.303C= (p.Cys101=) c.480C= (p.Cys160=) c.486-17031G= (n.486-17031G=) c.465C= (p.Cys155=) | |
9 | g.36246167G>T | CA373418497 | CLTA,GNE | c.573C>A (p.Cys191Ter) c.303C>A (p.Cys101Ter) c.480C>A (p.Cys160Ter) c.486-17031G>T (n.486-17031G>T) c.465C>A (p.Cys155Ter) | |
9 | g.36246168C>A | CA373418499 | CLTA,GNE | c.572G>T (p.Cys191Phe) c.302G>T (p.Cys101Phe) c.479G>T (p.Cys160Phe) c.486-17030C>A (n.486-17030C>A) c.464G>T (p.Cys155Phe) | |
9 | g.36246168C>G | CA373418501 | CLTA,GNE | c.572G>C (p.Cys191Ser) c.302G>C (p.Cys101Ser) c.479G>C (p.Cys160Ser) c.486-17030C>G (n.486-17030C>G) c.464G>C (p.Cys155Ser) | |
9 | g.36246168C>T | CA373418503 | CLTA,GNE | c.572G>A (p.Cys191Tyr) c.302G>A (p.Cys101Tyr) c.479G>A (p.Cys160Tyr) c.486-17030C>T (n.486-17030C>T) c.464G>A (p.Cys155Tyr) | |
9 | g.36246169A= | CA1846375313 | CLTA,GNE | c.571T= (p.Cys191=) c.301T= (p.Cys101=) c.478T= (p.Cys160=) c.486-17029A= (n.486-17029A=) c.463T= (p.Cys155=) | |
9 | g.36246169A>C | CA373418505 | CLTA,GNE | c.571T>G (p.Cys191Gly) c.301T>G (p.Cys101Gly) c.478T>G (p.Cys160Gly) c.486-17029A>C (n.486-17029A>C) c.463T>G (p.Cys155Gly) | |
9 | g.36246169A>G | CA373418507 | CLTA,GNE | c.571T>C (p.Cys191Arg) c.301T>C (p.Cys101Arg) c.478T>C (p.Cys160Arg) c.486-17029A>G (n.486-17029A>G) c.463T>C (p.Cys155Arg) | dbSNP gnomAD v2 |
9 | g.36246169A>T | CA373418509 | CLTA,GNE | c.571T>A (p.Cys191Ser) c.301T>A (p.Cys101Ser) c.478T>A (p.Cys160Ser) c.486-17029A>T (n.486-17029A>T) c.463T>A (p.Cys155Ser) | |
9 | g.36246170G>A | CA464619901 | CLTA,GNE | c.570C>T (p.Cys190=) c.300C>T (p.Cys100=) c.477C>T (p.Cys159=) c.486-17028G>A (n.486-17028G>A) c.462C>T (p.Cys154=) | gnomAD v4 |
9 | g.36246170G>C | CA373418511 | CLTA,GNE | c.570C>G (p.Cys190Trp) c.300C>G (p.Cys100Trp) c.477C>G (p.Cys159Trp) c.486-17028G>C (n.486-17028G>C) c.462C>G (p.Cys154Trp) | |
9 | g.36246170G>T | CA373418513 | CLTA,GNE | c.570C>A (p.Cys190Ter) c.300C>A (p.Cys100Ter) c.477C>A (p.Cys159Ter) c.486-17028G>T (n.486-17028G>T) c.462C>A (p.Cys154Ter) | |
9 | g.36246171C>A | CA373418515 | CLTA,GNE | c.569G>T (p.Cys190Phe) c.299G>T (p.Cys100Phe) c.476G>T (p.Cys159Phe) c.486-17027C>A (n.486-17027C>A) c.461G>T (p.Cys154Phe) | |
9 | g.36246171C>G | CA373418517 | CLTA,GNE | c.569G>C (p.Cys190Ser) c.299G>C (p.Cys100Ser) c.476G>C (p.Cys159Ser) c.486-17027C>G (n.486-17027C>G) c.461G>C (p.Cys154Ser) | ClinVar |
9 | g.36246171C>T | CA373418518 | CLTA,GNE | c.569G>A (p.Cys190Tyr) c.299G>A (p.Cys100Tyr) c.476G>A (p.Cys159Tyr) c.486-17027C>T (n.486-17027C>T) c.461G>A (p.Cys154Tyr) | |
9 | g.36246172A>C | CA373418522 | CLTA,GNE | c.568T>G (p.Cys190Gly) c.298T>G (p.Cys100Gly) c.475T>G (p.Cys159Gly) c.486-17026A>C (n.486-17026A>C) c.460T>G (p.Cys154Gly) | |
9 | g.36246172A>G | CA373418523 | CLTA,GNE | c.568T>C (p.Cys190Arg) c.298T>C (p.Cys100Arg) c.475T>C (p.Cys159Arg) c.486-17026A>G (n.486-17026A>G) c.460T>C (p.Cys154Arg) | gnomAD v4 COSMIC COSMIC COSMIC |
9 | g.36246172A>T | CA373418526 | CLTA,GNE | c.568T>A (p.Cys190Ser) c.298T>A (p.Cys100Ser) c.475T>A (p.Cys159Ser) c.486-17026A>T (n.486-17026A>T) c.460T>A (p.Cys154Ser) | |
9 | g.36246173C>A | CA464619907 | CLTA,GNE | c.567G>T (p.Val189=) c.297G>T (p.Val99=) c.474G>T (p.Val158=) c.486-17025C>A (n.486-17025C>A) c.459G>T (p.Val153=) | |
9 | g.36246173C= | CA1846375315 | CLTA,GNE | c.567G= (p.Val189=) c.297G= (p.Val99=) c.474G= (p.Val158=) c.486-17025C= (n.486-17025C=) c.459G= (p.Val153=) | |
9 | g.36246173C>G | CA5056723 | CLTA,GNE | c.567G>C (p.Val189=) c.297G>C (p.Val99=) c.474G>C (p.Val158=) c.486-17025C>G (n.486-17025C>G) c.459G>C (p.Val153=) | ClinVar dbSNP ExAC gnomAD v2 |
9 | g.36246173C>T | CA464619910 | CLTA,GNE | c.567G>A (p.Val189=) c.297G>A (p.Val99=) c.474G>A (p.Val158=) c.486-17025C>T (n.486-17025C>T) c.459G>A (p.Val153=) | ClinVar |
9 | g.36246174A>C | CA373418529 | CLTA,GNE | c.566T>G (p.Val189Gly) c.296T>G (p.Val99Gly) c.473T>G (p.Val158Gly) c.486-17024A>C (n.486-17024A>C) c.458T>G (p.Val153Gly) | |
9 | g.36246174A>G | CA373418530 | CLTA,GNE | c.566T>C (p.Val189Ala) c.296T>C (p.Val99Ala) c.473T>C (p.Val158Ala) c.486-17024A>G (n.486-17024A>G) c.458T>C (p.Val153Ala) | |
9 | g.36246174A>T | CA373418533 | CLTA,GNE | c.566T>A (p.Val189Glu) c.296T>A (p.Val99Glu) c.473T>A (p.Val158Glu) c.486-17024A>T (n.486-17024A>T) c.458T>A (p.Val153Glu) | |
9 | g.36246175C>A | CA373418535 | CLTA,GNE | c.565G>T (p.Val189Leu) c.295G>T (p.Val99Leu) c.472G>T (p.Val158Leu) c.486-17023C>A (n.486-17023C>A) c.457G>T (p.Val153Leu) | |
9 | g.36246175C>G | CA373418537 | CLTA,GNE | c.565G>C (p.Val189Leu) c.295G>C (p.Val99Leu) c.472G>C (p.Val158Leu) c.486-17023C>G (n.486-17023C>G) c.457G>C (p.Val153Leu) | |
9 | g.36246175C>T | CA373418539 | CLTA,GNE | c.565G>A (p.Val189Met) c.295G>A (p.Val99Met) c.472G>A (p.Val158Met) c.486-17023C>T (n.486-17023C>T) c.457G>A (p.Val153Met) | |
9 | g.36246175_36246177delinsCAT | CA1846375321 | CLTA,GNE | c.563_565delinsATG (p.His188=) c.293_295delinsATG (p.His98=) c.470_472delinsATG (p.His157=) c.486-17023_486-17021delinsCAT (n.486-17023_486-17021delinsCAT) c.455_457delinsATG (p.His152=) | |
9 | g.36246176A= | CA1846375327 | CLTA,GNE | c.564T= (p.His188=) c.294T= (p.His98=) c.471T= (p.His157=) c.486-17022A= (n.486-17022A=) c.456T= (p.His152=) | |
9 | g.36246176A>C | CA373418541 | CLTA,GNE | c.564T>G (p.His188Gln) c.294T>G (p.His98Gln) c.471T>G (p.His157Gln) c.486-17022A>C (n.486-17022A>C) c.456T>G (p.His152Gln) | |
9 | g.36246176A>G | CA5056724 | CLTA,GNE | c.564T>C (p.His188=) c.294T>C (p.His98=) c.471T>C (p.His157=) c.486-17022A>G (n.486-17022A>G) c.456T>C (p.His152=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.36246176A>T | CA373418544 | CLTA,GNE | c.564T>A (p.His188Gln) c.294T>A (p.His98Gln) c.471T>A (p.His157Gln) c.486-17022A>T (n.486-17022A>T) c.456T>A (p.His152Gln) | |
9 | g.36246176_36246177del | CA658797205 | CLTA,GNE | c.563_564del (p.His188ArgfsTer16) c.293_294del (p.His98ArgfsTer16) c.470_471del (p.His157ArgfsTer16) c.486-17022_486-17021del (n.486-17022_486-17021del) c.455_456del (p.His152ArgfsTer16) | ClinVar dbSNP gnomAD v4 |
9 | g.36246177T>A | CA373418546 | CLTA,GNE | c.563A>T (p.His188Leu) c.293A>T (p.His98Leu) c.470A>T (p.His157Leu) c.486-17021T>A (n.486-17021T>A) c.455A>T (p.His152Leu) | |
9 | g.36246177T>C | CA373418548 | CLTA,GNE | c.563A>G (p.His188Arg) c.293A>G (p.His98Arg) c.470A>G (p.His157Arg) c.486-17021T>C (n.486-17021T>C) c.455A>G (p.His152Arg) | |
9 | g.36246177T>G | CA373418550 | CLTA,GNE | c.563A>C (p.His188Pro) c.293A>C (p.His98Pro) c.470A>C (p.His157Pro) c.486-17021T>G (n.486-17021T>G) c.455A>C (p.His152Pro) | |
9 | g.36246178G>A | CA373418556 | CLTA,GNE | c.562C>T (p.His188Tyr) c.292C>T (p.His98Tyr) c.469C>T (p.His157Tyr) c.486-17020G>A (n.486-17020G>A) c.454C>T (p.His152Tyr) | ClinVar gnomAD v4 |
9 | g.36246178G>C | CA373418554 | CLTA,GNE | c.562C>G (p.His188Asp) c.292C>G (p.His98Asp) c.469C>G (p.His157Asp) c.486-17020G>C (n.486-17020G>C) c.454C>G (p.His152Asp) | |
9 | g.36246178G= | CA1846375332 | CLTA,GNE | c.562C= (p.His188=) c.292C= (p.His98=) c.469C= (p.His157=) c.486-17020G= (n.486-17020G=) c.454C= (p.His152=) | |
9 | g.36246178G>T | CA373418552 | CLTA,GNE | c.562C>A (p.His188Asn) c.292C>A (p.His98Asn) c.469C>A (p.His157Asn) c.486-17020G>T (n.486-17020G>T) c.454C>A (p.His152Asn) | ClinVar dbSNP |
9 | g.36246179A= | CA1846375334 | CLTA,GNE | c.561T= (p.Tyr187=) c.291T= (p.Tyr97=) c.468T= (p.Tyr156=) c.486-17019A= (n.486-17019A=) c.453T= (p.Tyr151=) | |
9 | g.36246179A>C | CA373418559 | CLTA,GNE | c.561T>G (p.Tyr187Ter) c.291T>G (p.Tyr97Ter) c.468T>G (p.Tyr156Ter) c.486-17019A>C (n.486-17019A>C) c.453T>G (p.Tyr151Ter) | |
9 | g.36246179A>G | CA464619919 | CLTA,GNE | c.561T>C (p.Tyr187=) c.291T>C (p.Tyr97=) c.468T>C (p.Tyr156=) c.486-17019A>G (n.486-17019A>G) c.453T>C (p.Tyr151=) | dbSNP |
9 | g.36246179A>T | CA373418560 | CLTA,GNE | c.561T>A (p.Tyr187Ter) c.291T>A (p.Tyr97Ter) c.468T>A (p.Tyr156Ter) c.486-17019A>T (n.486-17019A>T) c.453T>A (p.Tyr151Ter) | |
9 | g.36246180T>A | CA373418562 | CLTA,GNE | c.560A>T (p.Tyr187Phe) c.290A>T (p.Tyr97Phe) c.467A>T (p.Tyr156Phe) c.486-17018T>A (n.486-17018T>A) c.452A>T (p.Tyr151Phe) | |
9 | g.36246180T>C | CA373418564 | CLTA,GNE | c.560A>G (p.Tyr187Cys) c.290A>G (p.Tyr97Cys) c.467A>G (p.Tyr156Cys) c.486-17018T>C (n.486-17018T>C) c.452A>G (p.Tyr151Cys) | ClinVar dbSNP |
9 | g.36246180T>G | CA373418565 | CLTA,GNE | c.560A>C (p.Tyr187Ser) c.290A>C (p.Tyr97Ser) c.467A>C (p.Tyr156Ser) c.486-17018T>G (n.486-17018T>G) c.452A>C (p.Tyr151Ser) | |
9 | g.36246180dup | CA2689947823 | CLTA,GNE | c.560dup (p.Tyr187Ter) c.290dup (p.Tyr97Ter) c.467dup (p.Tyr156Ter) c.486-17018dup (n.486-17018dup) c.452dup (p.Tyr151Ter) | gnomAD v4 |
9 | g.36246181A= | CA1846375339 | CLTA,GNE | c.559T= (p.Tyr187=) c.289T= (p.Tyr97=) c.466T= (p.Tyr156=) c.486-17017A= (n.486-17017A=) c.451T= (p.Tyr151=) | |
9 | g.36246181A>C | CA373418567 | CLTA,GNE | c.559T>G (p.Tyr187Asp) c.289T>G (p.Tyr97Asp) c.466T>G (p.Tyr156Asp) c.486-17017A>C (n.486-17017A>C) c.451T>G (p.Tyr151Asp) | |
9 | g.36246181A>G | CA243356 | CLTA,GNE | c.559T>C (p.Tyr187His) c.289T>C (p.Tyr97His) c.466T>C (p.Tyr156His) c.486-17017A>G (n.486-17017A>G) c.451T>C (p.Tyr151His) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
9 | g.36246181A>T | CA373418570 | CLTA,GNE | c.559T>A (p.Tyr187Asn) c.289T>A (p.Tyr97Asn) c.466T>A (p.Tyr156Asn) c.486-17017A>T (n.486-17017A>T) c.451T>A (p.Tyr151Asn) | |
9 | g.36246182A>C | CA373418572 | CLTA,GNE | c.558T>G (p.His186Gln) c.288T>G (p.His96Gln) c.465T>G (p.His155Gln) c.486-17016A>C (n.486-17016A>C) c.450T>G (p.His150Gln) | |
9 | g.36246182A>G | CA464619925 | CLTA,GNE | c.558T>C (p.His186=) c.288T>C (p.His96=) c.465T>C (p.His155=) c.486-17016A>G (n.486-17016A>G) c.450T>C (p.His150=) | gnomAD v4 |
9 | g.36246182A>T | CA373418573 | CLTA,GNE | c.558T>A (p.His186Gln) c.288T>A (p.His96Gln) c.465T>A (p.His155Gln) c.486-17016A>T (n.486-17016A>T) c.450T>A (p.His150Gln) | |
9 | g.36246183T>A | CA373418575 | CLTA,GNE | c.557A>T (p.His186Leu) c.287A>T (p.His96Leu) c.464A>T (p.His155Leu) c.486-17015T>A (n.486-17015T>A) c.449A>T (p.His150Leu) | |
9 | g.36246183T>C | CA373418577 | CLTA,GNE | c.557A>G (p.His186Arg) c.287A>G (p.His96Arg) c.464A>G (p.His155Arg) c.486-17015T>C (n.486-17015T>C) c.449A>G (p.His150Arg) | |
9 | g.36246183T>G | CA373418579 | CLTA,GNE | c.557A>C (p.His186Pro) c.287A>C (p.His96Pro) c.464A>C (p.His155Pro) c.486-17015T>G (n.486-17015T>G) c.449A>C (p.His150Pro) | |
9 | g.36246183T= | CA1846375341 | CLTA,GNE | c.557A= (p.His186=) c.287A= (p.His96=) c.464A= (p.His155=) c.486-17015T= (n.486-17015T=) c.449A= (p.His150=) | |
9 | g.36246184G>A | CA373418585 | CLTA,GNE | c.556C>T (p.His186Tyr) c.286C>T (p.His96Tyr) c.463C>T (p.His155Tyr) c.486-17014G>A (n.486-17014G>A) c.448C>T (p.His150Tyr) | gnomAD v4 |
9 | g.36246184G>C | CA373418581 | CLTA,GNE | c.556C>G (p.His186Asp) c.286C>G (p.His96Asp) c.463C>G (p.His155Asp) c.486-17014G>C (n.486-17014G>C) c.448C>G (p.His150Asp) | |
9 | g.36246184G>T | CA373418583 | CLTA,GNE | c.556C>A (p.His186Asn) c.286C>A (p.His96Asn) c.463C>A (p.His155Asn) c.486-17014G>T (n.486-17014G>T) c.448C>A (p.His150Asn) | |
9 | g.36246184dup | CA1846375343 | CLTA,GNE | c.556dup (p.His186ProfsTer19) c.286dup (p.His96ProfsTer19) c.463dup (p.His155ProfsTer19) c.486-17014dup (n.486-17014dup) c.448dup (p.His150ProfsTer19) | dbSNP |
9 | g.36246185A= | CA1846375351 | CLTA,GNE | c.555T= (p.Ala185=) c.285T= (p.Ala95=) c.462T= (p.Ala154=) c.486-17013A= (n.486-17013A=) c.447T= (p.Ala149=) | |
9 | g.36246185A>C | CA464619926 | CLTA,GNE | c.555T>G (p.Ala185=) c.285T>G (p.Ala95=) c.462T>G (p.Ala154=) c.486-17013A>C (n.486-17013A>C) c.447T>G (p.Ala149=) | |
9 | g.36246185A>G | CA464619927 | CLTA,GNE | c.555T>C (p.Ala185=) c.285T>C (p.Ala95=) c.462T>C (p.Ala154=) c.486-17013A>G (n.486-17013A>G) c.447T>C (p.Ala149=) | |
9 | g.36246185A>T | CA5056725 | CLTA,GNE | c.555T>A (p.Ala185=) c.285T>A (p.Ala95=) c.462T>A (p.Ala154=) c.486-17013A>T (n.486-17013A>T) c.447T>A (p.Ala149=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.36246186G>A | CA373418589 | CLTA,GNE | c.554C>T (p.Ala185Val) c.284C>T (p.Ala95Val) c.461C>T (p.Ala154Val) c.486-17012G>A (n.486-17012G>A) c.446C>T (p.Ala149Val) | |
9 | g.36246186G>C | CA373418591 | CLTA,GNE | c.554C>G (p.Ala185Gly) c.284C>G (p.Ala95Gly) c.461C>G (p.Ala154Gly) c.486-17012G>C (n.486-17012G>C) c.446C>G (p.Ala149Gly) | |
9 | g.36246186G>T | CA373418592 | CLTA,GNE | c.554C>A (p.Ala185Asp) c.284C>A (p.Ala95Asp) c.461C>A (p.Ala154Asp) c.486-17012G>T (n.486-17012G>T) c.446C>A (p.Ala149Asp) | |
9 | g.36246187C>A | CA373418595 | CLTA,GNE | c.553G>T (p.Ala185Ser) c.283G>T (p.Ala95Ser) c.460G>T (p.Ala154Ser) c.486-17011C>A (n.486-17011C>A) c.445G>T (p.Ala149Ser) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.36246187C= | CA1846375370 | CLTA,GNE | c.553G= (p.Ala185=) c.283G= (p.Ala95=) c.460G= (p.Ala154=) c.486-17011C= (n.486-17011C=) c.445G= (p.Ala149=) | |
9 | g.36246187C>G | CA373418597 | CLTA,GNE | c.553G>C (p.Ala185Pro) c.283G>C (p.Ala95Pro) c.460G>C (p.Ala154Pro) c.486-17011C>G (n.486-17011C>G) c.445G>C (p.Ala149Pro) | |
9 | g.36246187C>T | CA373418599 | CLTA,GNE | c.553G>A (p.Ala185Thr) c.283G>A (p.Ala95Thr) c.460G>A (p.Ala154Thr) c.486-17011C>T (n.486-17011C>T) c.445G>A (p.Ala149Thr) | |
9 | g.36246188C>A | CA464619931 | CLTA,GNE | c.552G>T (p.Leu184=) c.282G>T (p.Leu94=) c.459G>T (p.Leu153=) c.486-17010C>A (n.486-17010C>A) c.444G>T (p.Leu148=) | gnomAD v4 |
9 | g.36246188C= | CA1846375373 | CLTA,GNE | c.552G= (p.Leu184=) c.282G= (p.Leu94=) c.459G= (p.Leu153=) c.486-17010C= (n.486-17010C=) c.444G= (p.Leu148=) | |
9 | g.36246188C>G | CA464619932 | CLTA,GNE | c.552G>C (p.Leu184=) c.282G>C (p.Leu94=) c.459G>C (p.Leu153=) c.486-17010C>G (n.486-17010C>G) c.444G>C (p.Leu148=) | |
9 | g.36246188C>T | CA464619933 | CLTA,GNE | c.552G>A (p.Leu184=) c.282G>A (p.Leu94=) c.459G>A (p.Leu153=) c.486-17010C>T (n.486-17010C>T) c.444G>A (p.Leu148=) | dbSNP gnomAD v3 gnomAD v4 |
9 | g.36246189A>C | CA373418600 | CLTA,GNE | c.551T>G (p.Leu184Arg) c.281T>G (p.Leu94Arg) c.458T>G (p.Leu153Arg) c.486-17009A>C (n.486-17009A>C) c.443T>G (p.Leu148Arg) | |
9 | g.36246189A>G | CA373418602 | CLTA,GNE | c.551T>C (p.Leu184Pro) c.281T>C (p.Leu94Pro) c.458T>C (p.Leu153Pro) c.486-17009A>G (n.486-17009A>G) c.443T>C (p.Leu148Pro) | gnomAD v4 |
9 | g.36246189A>T | CA373418604 | CLTA,GNE | c.551T>A (p.Leu184Gln) c.281T>A (p.Leu94Gln) c.458T>A (p.Leu153Gln) c.486-17009A>T (n.486-17009A>T) c.443T>A (p.Leu148Gln) | |
9 | g.36246190G>A | CA464619937 | CLTA,GNE | c.550C>T (p.Leu184=) c.280C>T (p.Leu94=) c.457C>T (p.Leu153=) c.486-17008G>A (n.486-17008G>A) c.442C>T (p.Leu148=) | COSMIC COSMIC COSMIC |
9 | g.36246190G>C | CA373418606 | CLTA,GNE | c.550C>G (p.Leu184Val) c.280C>G (p.Leu94Val) c.457C>G (p.Leu153Val) c.486-17008G>C (n.486-17008G>C) c.442C>G (p.Leu148Val) | |
9 | g.36246190G= | CA1846375376 | CLTA,GNE | c.550C= (p.Leu184=) c.280C= (p.Leu94=) c.457C= (p.Leu153=) c.486-17008G= (n.486-17008G=) c.442C= (p.Leu148=) | |
9 | g.36246190G>T | CA373418607 | CLTA,GNE | c.550C>A (p.Leu184Met) c.280C>A (p.Leu94Met) c.457C>A (p.Leu153Met) c.486-17008G>T (n.486-17008G>T) c.442C>A (p.Leu148Met) | |
9 | g.36246191T>A | CA373418610 | CLTA,GNE | c.549A>T (p.Lys183Asn) c.279A>T (p.Lys93Asn) c.456A>T (p.Lys152Asn) c.486-17007T>A (n.486-17007T>A) c.441A>T (p.Lys147Asn) | |
9 | g.36246191T>C | CA464619939 | CLTA,GNE | c.549A>G (p.Lys183=) c.279A>G (p.Lys93=) c.456A>G (p.Lys152=) c.486-17007T>C (n.486-17007T>C) c.441A>G (p.Lys147=) | |
9 | g.36246191T>G | CA373418608 | CLTA,GNE | c.549A>C (p.Lys183Asn) c.279A>C (p.Lys93Asn) c.456A>C (p.Lys152Asn) c.486-17007T>G (n.486-17007T>G) c.441A>C (p.Lys147Asn) | |
9 | g.36246194dup | CA918447763 | CLTA,GNE | c.549dup (p.Leu184ThrfsTer21) c.279dup (p.Leu94ThrfsTer21) c.456dup (p.Leu153ThrfsTer21) c.486-17004dup (n.486-17004dup) c.441dup (p.Leu148ThrfsTer21) | dbSNP gnomAD v4 |
9 | g.36246192T>A | CA373418613 | CLTA,GNE | c.548A>T (p.Lys183Ile) c.278A>T (p.Lys93Ile) c.455A>T (p.Lys152Ile) c.486-17006T>A (n.486-17006T>A) c.440A>T (p.Lys147Ile) | |
9 | g.36246192T>C | CA373418616 | CLTA,GNE | c.548A>G (p.Lys183Arg) c.278A>G (p.Lys93Arg) c.455A>G (p.Lys152Arg) c.486-17006T>C (n.486-17006T>C) c.440A>G (p.Lys147Arg) | |
9 | g.36246192T>G | CA373418614 | CLTA,GNE | c.548A>C (p.Lys183Thr) c.278A>C (p.Lys93Thr) c.455A>C (p.Lys152Thr) c.486-17006T>G (n.486-17006T>G) c.440A>C (p.Lys147Thr) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
9 | g.36246192T= | CA1846375383 | CLTA,GNE | c.548A= (p.Lys183=) c.278A= (p.Lys93=) c.455A= (p.Lys152=) c.486-17006T= (n.486-17006T=) c.440A= (p.Lys147=) | |
9 | g.36246193T>A | CA373418619 | CLTA,GNE | c.547A>T (p.Lys183Ter) c.277A>T (p.Lys93Ter) c.454A>T (p.Lys152Ter) c.486-17005T>A (n.486-17005T>A) c.439A>T (p.Lys147Ter) | |
9 | g.36246193T>C | CA373418621 | CLTA,GNE | c.547A>G (p.Lys183Glu) c.277A>G (p.Lys93Glu) c.454A>G (p.Lys152Glu) c.486-17005T>C (n.486-17005T>C) c.439A>G (p.Lys147Glu) | gnomAD v4 |
9 | g.36246193T>G | CA373418620 | CLTA,GNE | c.547A>C (p.Lys183Gln) c.277A>C (p.Lys93Gln) c.454A>C (p.Lys152Gln) c.486-17005T>G (n.486-17005T>G) c.439A>C (p.Lys147Gln) | |
9 | g.36246194T>A | CA464619948 | CLTA,GNE | c.546A>T (p.Thr182=) c.276A>T (p.Thr92=) c.453A>T (p.Thr151=) c.486-17004T>A (n.486-17004T>A) c.438A>T (p.Thr146=) | |
9 | g.36246194T>C | CA464619949 | CLTA,GNE | c.546A>G (p.Thr182=) c.276A>G (p.Thr92=) c.453A>G (p.Thr151=) c.486-17004T>C (n.486-17004T>C) c.438A>G (p.Thr146=) | |
9 | g.36246194T>G | CA464619950 | CLTA,GNE | c.546A>C (p.Thr182=) c.276A>C (p.Thr92=) c.453A>C (p.Thr151=) c.486-17004T>G (n.486-17004T>G) c.438A>C (p.Thr146=) | |
9 | g.36246195G>A | CA373418622 | CLTA,GNE | c.545C>T (p.Thr182Ile) c.275C>T (p.Thr92Ile) c.452C>T (p.Thr151Ile) c.486-17003G>A (n.486-17003G>A) c.437C>T (p.Thr146Ile) | gnomAD v4 |
9 | g.36246195G>C | CA373418623 | CLTA,GNE | c.545C>G (p.Thr182Arg) c.275C>G (p.Thr92Arg) c.452C>G (p.Thr151Arg) c.486-17003G>C (n.486-17003G>C) c.437C>G (p.Thr146Arg) | |
9 | g.36246195G>T | CA373418625 | CLTA,GNE | c.545C>A (p.Thr182Lys) c.275C>A (p.Thr92Lys) c.452C>A (p.Thr151Lys) c.486-17003G>T (n.486-17003G>T) c.437C>A (p.Thr146Lys) | |
9 | g.36246196T>A | CA373418627 | CLTA,GNE | c.544A>T (p.Thr182Ser) c.274A>T (p.Thr92Ser) c.451A>T (p.Thr151Ser) c.486-17002T>A (n.486-17002T>A) c.436A>T (p.Thr146Ser) | |
9 | g.36246196T>C | CA373418629 | CLTA,GNE | c.544A>G (p.Thr182Ala) c.274A>G (p.Thr92Ala) c.451A>G (p.Thr151Ala) c.486-17002T>C (n.486-17002T>C) c.436A>G (p.Thr146Ala) | |
9 | g.36246196T>G | CA373418631 | CLTA,GNE | c.544A>C (p.Thr182Pro) c.274A>C (p.Thr92Pro) c.451A>C (p.Thr151Pro) c.486-17002T>G (n.486-17002T>G) c.436A>C (p.Thr146Pro) | |
9 | g.36246197T>A | CA464619957 | CLTA,GNE | c.543A>T (p.Ile181=) c.273A>T (p.Ile91=) c.450A>T (p.Ile150=) c.486-17001T>A (n.486-17001T>A) c.435A>T (p.Ile145=) | dbSNP gnomAD v4 |
9 | g.36246197T>C | CA373418632 | CLTA,GNE | c.543A>G (p.Ile181Met) c.273A>G (p.Ile91Met) c.450A>G (p.Ile150Met) c.486-17001T>C (n.486-17001T>C) c.435A>G (p.Ile145Met) | |
9 | g.36246197T>G | CA464619956 | CLTA,GNE | c.543A>C (p.Ile181=) c.273A>C (p.Ile91=) c.450A>C (p.Ile150=) c.486-17001T>G (n.486-17001T>G) c.435A>C (p.Ile145=) | |
9 | g.36246197T= | CA1846375388 | CLTA,GNE | c.543A= (p.Ile181=) c.273A= (p.Ile91=) c.450A= (p.Ile150=) c.486-17001T= (n.486-17001T=) c.435A= (p.Ile145=) | |
9 | g.36246198A= | CA1846375390 | CLTA,GNE | c.542T= (p.Ile181=) c.272T= (p.Ile91=) c.449T= (p.Ile150=) c.486-17000A= (n.486-17000A=) c.434T= (p.Ile145=) | |
9 | g.36246198A>C | CA373418634 | CLTA,GNE | c.542T>G (p.Ile181Arg) c.272T>G (p.Ile91Arg) c.449T>G (p.Ile150Arg) c.486-17000A>C (n.486-17000A>C) c.434T>G (p.Ile145Arg) | |
9 | g.36246198A>G | CA373418636 | CLTA,GNE | c.542T>C (p.Ile181Thr) c.272T>C (p.Ile91Thr) c.449T>C (p.Ile150Thr) c.486-17000A>G (n.486-17000A>G) c.434T>C (p.Ile145Thr) | |
9 | g.36246198A>T | CA5056726 | CLTA,GNE | c.542T>A (p.Ile181Lys) c.272T>A (p.Ile91Lys) c.449T>A (p.Ile150Lys) c.486-17000A>T (n.486-17000A>T) c.434T>A (p.Ile145Lys) | dbSNP ExAC gnomAD v2 gnomAD v4 |
9 | g.36246199T>A | CA5056727 | CLTA,GNE | c.541A>T (p.Ile181Leu) c.271A>T (p.Ile91Leu) c.448A>T (p.Ile150Leu) c.486-16999T>A (n.486-16999T>A) c.433A>T (p.Ile145Leu) | dbSNP ExAC gnomAD v2 gnomAD v4 |
9 | g.36246199T>C | CA373418640 | CLTA,GNE | c.541A>G (p.Ile181Val) c.271A>G (p.Ile91Val) c.448A>G (p.Ile150Val) c.486-16999T>C (n.486-16999T>C) c.433A>G (p.Ile145Val) | ClinVar dbSNP COSMIC COSMIC COSMIC |
9 | g.36246199T>G | CA373418639 | CLTA,GNE | c.541A>C (p.Ile181Leu) c.271A>C (p.Ile91Leu) c.448A>C (p.Ile150Leu) c.486-16999T>G (n.486-16999T>G) c.433A>C (p.Ile145Leu) | |
9 | g.36246199T= | CA1846375399 | CLTA,GNE | c.541A= (p.Ile181=) c.271A= (p.Ile91=) c.448A= (p.Ile150=) c.486-16999T= (n.486-16999T=) c.433A= (p.Ile145=) | |
9 | g.36246200G>A | CA5056728 | CLTA,GNE | c.540C>T (p.Ala180=) c.270C>T (p.Ala90=) c.447C>T (p.Ala149=) c.486-16998G>A (n.486-16998G>A) c.432C>T (p.Ala144=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
9 | g.36246200G>C | CA464619962 | CLTA,GNE | c.540C>G (p.Ala180=) c.270C>G (p.Ala90=) c.447C>G (p.Ala149=) c.486-16998G>C (n.486-16998G>C) c.432C>G (p.Ala144=) | |
9 | g.36246200G= | CA1846375401 | CLTA,GNE | c.540C= (p.Ala180=) c.270C= (p.Ala90=) c.447C= (p.Ala149=) c.486-16998G= (n.486-16998G=) c.432C= (p.Ala144=) | |
9 | g.36246200G>T | CA464619961 | CLTA,GNE | c.540C>A (p.Ala180=) c.270C>A (p.Ala90=) c.447C>A (p.Ala149=) c.486-16998G>T (n.486-16998G>T) c.432C>A (p.Ala144=) | |
9 | g.36246201G>A | CA373418644 | CLTA,GNE | c.539C>T (p.Ala180Val) c.269C>T (p.Ala90Val) c.446C>T (p.Ala149Val) c.486-16997G>A (n.486-16997G>A) c.431C>T (p.Ala144Val) | |
9 | g.36246201G>C | CA373418645 | CLTA,GNE | c.539C>G (p.Ala180Gly) c.269C>G (p.Ala90Gly) c.446C>G (p.Ala149Gly) c.486-16997G>C (n.486-16997G>C) c.431C>G (p.Ala144Gly) | |
9 | g.36246201G= | CA1846375405 | CLTA,GNE | c.539C= (p.Ala180=) c.269C= (p.Ala90=) c.446C= (p.Ala149=) c.486-16997G= (n.486-16997G=) c.431C= (p.Ala144=) | |
9 | g.36246201G>T | CA5056729 | CLTA,GNE | c.539C>A (p.Ala180Asp) c.269C>A (p.Ala90Asp) c.446C>A (p.Ala149Asp) c.486-16997G>T (n.486-16997G>T) c.431C>A (p.Ala144Asp) | dbSNP ExAC gnomAD v2 |
9 | g.36246202C>A | CA373418649 | CLTA,GNE | c.538G>T (p.Ala180Ser) c.268G>T (p.Ala90Ser) c.445G>T (p.Ala149Ser) c.486-16996C>A (n.486-16996C>A) c.430G>T (p.Ala144Ser) | ClinVar dbSNP |
9 | g.36246202C= | CA1846375410 | CLTA,GNE | c.538G= (p.Ala180=) c.268G= (p.Ala90=) c.445G= (p.Ala149=) c.486-16996C= (n.486-16996C=) c.430G= (p.Ala144=) | |
9 | g.36246202C>G | CA373418651 | CLTA,GNE | c.538G>C (p.Ala180Pro) c.268G>C (p.Ala90Pro) c.445G>C (p.Ala149Pro) c.486-16996C>G (n.486-16996C>G) c.430G>C (p.Ala144Pro) | |
9 | g.36246202C>T | CA373418653 | CLTA,GNE | c.538G>A (p.Ala180Thr) c.268G>A (p.Ala90Thr) c.445G>A (p.Ala149Thr) c.486-16996C>T (n.486-16996C>T) c.430G>A (p.Ala144Thr) | |
9 | g.36246203A>C | CA373418655 | CLTA,GNE | c.537T>G (p.His179Gln) c.267T>G (p.His89Gln) c.444T>G (p.His148Gln) c.486-16995A>C (n.486-16995A>C) c.429T>G (p.His143Gln) | |
9 | g.36246203A>G | CA464619966 | CLTA,GNE | c.537T>C (p.His179=) c.267T>C (p.His89=) c.444T>C (p.His148=) c.486-16995A>G (n.486-16995A>G) c.429T>C (p.His143=) | ClinVar gnomAD v4 |
9 | g.36246203A>T | CA373418657 | CLTA,GNE | c.537T>A (p.His179Gln) c.267T>A (p.His89Gln) c.444T>A (p.His148Gln) c.486-16995A>T (n.486-16995A>T) c.429T>A (p.His143Gln) | |
9 | g.36246204T>A | CA373418660 | CLTA,GNE | c.536A>T (p.His179Leu) c.266A>T (p.His89Leu) c.443A>T (p.His148Leu) c.486-16994T>A (n.486-16994T>A) c.428A>T (p.His143Leu) | |
9 | g.36246204T>C | CA373418662 | CLTA,GNE | c.536A>G (p.His179Arg) c.266A>G (p.His89Arg) c.443A>G (p.His148Arg) c.486-16994T>C (n.486-16994T>C) c.428A>G (p.His143Arg) | ClinVar |
9 | g.36246204T>G | CA373418663 | CLTA,GNE | c.536A>C (p.His179Pro) c.266A>C (p.His89Pro) c.443A>C (p.His148Pro) c.486-16994T>G (n.486-16994T>G) c.428A>C (p.His143Pro) | |
9 | g.36246205G>A | CA373418668 | CLTA,GNE | c.535C>T (p.His179Tyr) c.265C>T (p.His89Tyr) c.442C>T (p.His148Tyr) c.486-16993G>A (n.486-16993G>A) c.427C>T (p.His143Tyr) | gnomAD v4 |
9 | g.36246205G>C | CA373418670 | CLTA,GNE | c.535C>G (p.His179Asp) c.265C>G (p.His89Asp) c.442C>G (p.His148Asp) c.486-16993G>C (n.486-16993G>C) c.427C>G (p.His143Asp) | |
9 | g.36246205G>T | CA373418666 | CLTA,GNE | c.535C>A (p.His179Asn) c.265C>A (p.His89Asn) c.442C>A (p.His148Asn) c.486-16993G>T (n.486-16993G>T) c.427C>A (p.His143Asn) | |
9 | g.36246206T>A | CA373418672 | CLTA,GNE | c.534A>T (p.Arg178Ser) c.264A>T (p.Arg88Ser) c.441A>T (p.Arg147Ser) c.486-16992T>A (n.486-16992T>A) c.426A>T (p.Arg142Ser) | |
9 | g.36246206T>C | CA464619969 | CLTA,GNE | c.534A>G (p.Arg178=) c.264A>G (p.Arg88=) c.441A>G (p.Arg147=) c.486-16992T>C (n.486-16992T>C) c.426A>G (p.Arg142=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
9 | g.36246206T>G | CA373418673 | CLTA,GNE | c.534A>C (p.Arg178Ser) c.264A>C (p.Arg88Ser) c.441A>C (p.Arg147Ser) c.486-16992T>G (n.486-16992T>G) c.426A>C (p.Arg142Ser) | |
9 | g.36246206T= | CA1846375415 | CLTA,GNE | c.534A= (p.Arg178=) c.264A= (p.Arg88=) c.441A= (p.Arg147=) c.486-16992T= (n.486-16992T=) c.426A= (p.Arg142=) | |
9 | g.36246207C>A | CA373418676 | CLTA,GNE | c.533G>T (p.Arg178Ile) c.263G>T (p.Arg88Ile) c.440G>T (p.Arg147Ile) c.486-16991C>A (n.486-16991C>A) c.425G>T (p.Arg142Ile) | |
9 | g.36246207C>G | CA373418677 | CLTA,GNE | c.533G>C (p.Arg178Thr) c.263G>C (p.Arg88Thr) c.440G>C (p.Arg147Thr) c.486-16991C>G (n.486-16991C>G) c.425G>C (p.Arg142Thr) | |
9 | g.36246207C>T | CA373418679 | CLTA,GNE | c.533G>A (p.Arg178Lys) c.263G>A (p.Arg88Lys) c.440G>A (p.Arg147Lys) c.486-16991C>T (n.486-16991C>T) c.425G>A (p.Arg142Lys) | |
9 | g.36246208T>A | CA373418681 | CLTA,GNE | c.532A>T (p.Arg178Ter) c.262A>T (p.Arg88Ter) c.439A>T (p.Arg147Ter) c.486-16990T>A (n.486-16990T>A) c.424A>T (p.Arg142Ter) | |
9 | g.36246208T>C | CA373418683 | CLTA,GNE | c.532A>G (p.Arg178Gly) c.262A>G (p.Arg88Gly) c.439A>G (p.Arg147Gly) c.486-16990T>C (n.486-16990T>C) c.424A>G (p.Arg142Gly) | gnomAD v4 |
9 | g.36246208T>G | CA464619970 | CLTA,GNE | c.532A>C (p.Arg178=) c.262A>C (p.Arg88=) c.439A>C (p.Arg147=) c.486-16990T>G (n.486-16990T>G) c.424A>C (p.Arg142=) | |
9 | g.36246208_36246212delinsTGATA | CA1846375418 | CLTA,GNE | c.528_532delinsTATCA (p.Ser176=) c.258_262delinsTATCA (p.Ser86=) c.435_439delinsTATCA (p.Ser145=) c.486-16990_486-16986delinsTGATA (n.486-16990_486-16986delinsTGATA) c.420_424delinsTATCA (p.Ser140=) | |
9 | g.36246209G>A | CA464619974 | CLTA,GNE | c.531C>T (p.Ile177=) c.261C>T (p.Ile87=) c.438C>T (p.Ile146=) c.486-16989G>A (n.486-16989G>A) c.423C>T (p.Ile141=) | |
9 | g.36246209G>C | CA373418685 | CLTA,GNE | c.531C>G (p.Ile177Met) c.261C>G (p.Ile87Met) c.438C>G (p.Ile146Met) c.486-16989G>C (n.486-16989G>C) c.423C>G (p.Ile141Met) | COSMIC COSMIC COSMIC |
9 | g.36246209G>T | CA464619976 | CLTA,GNE | c.531C>A (p.Ile177=) c.261C>A (p.Ile87=) c.438C>A (p.Ile146=) c.486-16989G>T (n.486-16989G>T) c.423C>A (p.Ile141=) | |
9 | g.36246211_36246214del | CA16041322 | CLTA,GNE | c.528_531del (p.Ile177AspfsTer4) c.258_261del (p.Ile87AspfsTer4) c.435_438del (p.Ile146AspfsTer4) c.486-16987_486-16984del (n.486-16987_486-16984del) c.420_423del (p.Ile141AspfsTer4) | ClinVar dbSNP |
9 | g.36246210A>C | CA373418689 | CLTA,GNE | c.530T>G (p.Ile177Ser) c.260T>G (p.Ile87Ser) c.437T>G (p.Ile146Ser) c.486-16988A>C (n.486-16988A>C) c.422T>G (p.Ile141Ser) | |
9 | g.36246210A>G | CA373418690 | CLTA,GNE | c.530T>C (p.Ile177Thr) c.260T>C (p.Ile87Thr) c.437T>C (p.Ile146Thr) c.486-16988A>G (n.486-16988A>G) c.422T>C (p.Ile141Thr) | |
9 | g.36246210A>T | CA373418692 | CLTA,GNE | c.530T>A (p.Ile177Asn) c.260T>A (p.Ile87Asn) c.437T>A (p.Ile146Asn) c.486-16988A>T (n.486-16988A>T) c.422T>A (p.Ile141Asn) | |
9 | g.36246210_36246211delinsAT | CA1846375426 | CLTA,GNE | c.529_530delinsAT (p.Ile177=) c.259_260delinsAT (p.Ile87=) c.436_437delinsAT (p.Ile146=) c.486-16988_486-16987delinsAT (n.486-16988_486-16987delinsAT) c.421_422delinsAT (p.Ile141=) | |
9 | g.36246211del | CA1123252950 | CLTA,GNE | c.529del (p.Ile177SerfsTer5) c.259del (p.Ile87SerfsTer5) c.436del (p.Ile146SerfsTer5) c.486-16987del (n.486-16987del) c.421del (p.Ile141SerfsTer5) | dbSNP gnomAD v3 gnomAD v4 |
9 | g.36246211T>A | CA373418696 | CLTA,GNE | c.529A>T (p.Ile177Phe) c.259A>T (p.Ile87Phe) c.436A>T (p.Ile146Phe) c.486-16987T>A (n.486-16987T>A) c.421A>T (p.Ile141Phe) | |
9 | g.36246211T>C | CA373418698 | CLTA,GNE | c.529A>G (p.Ile177Val) c.259A>G (p.Ile87Val) c.436A>G (p.Ile146Val) c.486-16987T>C (n.486-16987T>C) c.421A>G (p.Ile141Val) | ClinVar dbSNP |
9 | g.36246211T>G | CA373418695 | CLTA,GNE | c.529A>C (p.Ile177Leu) c.259A>C (p.Ile87Leu) c.436A>C (p.Ile146Leu) c.486-16987T>G (n.486-16987T>G) c.421A>C (p.Ile141Leu) | |
9 | g.36246212A= | CA1846375430 | CLTA,GNE | c.528T= (p.Ser176=) c.258T= (p.Ser86=) c.435T= (p.Ser145=) c.486-16986A= (n.486-16986A=) c.420T= (p.Ser140=) | |
9 | g.36246212A>C | CA464619981 | CLTA,GNE | c.528T>G (p.Ser176=) c.258T>G (p.Ser86=) c.435T>G (p.Ser145=) c.486-16986A>C (n.486-16986A>C) c.420T>G (p.Ser140=) | |
9 | g.36246212A>G | CA5056730 | CLTA,GNE | c.528T>C (p.Ser176=) c.258T>C (p.Ser86=) c.435T>C (p.Ser145=) c.486-16986A>G (n.486-16986A>G) c.420T>C (p.Ser140=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
9 | g.36246212A>T | CA464619983 | CLTA,GNE | c.528T>A (p.Ser176=) c.258T>A (p.Ser86=) c.435T>A (p.Ser145=) c.486-16986A>T (n.486-16986A>T) c.420T>A (p.Ser140=) | |
9 | g.36246212dup | CA2689947824 | CLTA,GNE | c.528dup (p.Ile177TyrfsTer28) c.258dup (p.Ile87TyrfsTer28) c.435dup (p.Ile146TyrfsTer28) c.486-16986dup (n.486-16986dup) c.420dup (p.Ile141TyrfsTer28) | gnomAD v4 |
9 | g.36246213G>A | CA373418702 | CLTA,GNE | c.527C>T (p.Ser176Phe) c.257C>T (p.Ser86Phe) c.434C>T (p.Ser145Phe) c.486-16985G>A (n.486-16985G>A) c.419C>T (p.Ser140Phe) | |
9 | g.36246213G>C | CA373418704 | CLTA,GNE | c.527C>G (p.Ser176Cys) c.257C>G (p.Ser86Cys) c.434C>G (p.Ser145Cys) c.486-16985G>C (n.486-16985G>C) c.419C>G (p.Ser140Cys) | |
9 | g.36246213G>T | CA373418706 | CLTA,GNE | c.527C>A (p.Ser176Tyr) c.257C>A (p.Ser86Tyr) c.434C>A (p.Ser145Tyr) c.486-16985G>T (n.486-16985G>T) c.419C>A (p.Ser140Tyr) | |
9 | g.36246214A>C | CA373418708 | CLTA,GNE | c.526T>G (p.Ser176Ala) c.256T>G (p.Ser86Ala) c.433T>G (p.Ser145Ala) c.486-16984A>C (n.486-16984A>C) c.418T>G (p.Ser140Ala) | gnomAD v4 |
9 | g.36246214A>G | CA373418711 | CLTA,GNE | c.526T>C (p.Ser176Pro) c.256T>C (p.Ser86Pro) c.433T>C (p.Ser145Pro) c.486-16984A>G (n.486-16984A>G) c.418T>C (p.Ser140Pro) | |
9 | g.36246214A>T | CA373418712 | CLTA,GNE | c.526T>A (p.Ser176Thr) c.256T>A (p.Ser86Thr) c.433T>A (p.Ser145Thr) c.486-16984A>T (n.486-16984A>T) c.418T>A (p.Ser140Thr) | |
9 | g.36246215G>A | CA464619988 | CLTA,GNE | c.525C>T (p.Asp175=) c.255C>T (p.Asp85=) c.432C>T (p.Asp144=) c.486-16983G>A (n.486-16983G>A) c.417C>T (p.Asp139=) | ClinVar dbSNP |
9 | g.36246215G>C | CA373418714 | CLTA,GNE | c.525C>G (p.Asp175Glu) c.255C>G (p.Asp85Glu) c.432C>G (p.Asp144Glu) c.486-16983G>C (n.486-16983G>C) c.417C>G (p.Asp139Glu) | |
9 | g.36246215G>T | CA373418716 | CLTA,GNE | c.525C>A (p.Asp175Glu) c.255C>A (p.Asp85Glu) c.432C>A (p.Asp144Glu) c.486-16983G>T (n.486-16983G>T) c.417C>A (p.Asp139Glu) | |
9 | g.36246216T>A | CA373418718 | CLTA,GNE | c.524A>T (p.Asp175Val) c.254A>T (p.Asp85Val) c.431A>T (p.Asp144Val) c.486-16982T>A (n.486-16982T>A) c.416A>T (p.Asp139Val) | |
9 | g.36246216T>C | CA373418720 | CLTA,GNE | c.524A>G (p.Asp175Gly) c.254A>G (p.Asp85Gly) c.431A>G (p.Asp144Gly) c.486-16982T>C (n.486-16982T>C) c.416A>G (p.Asp139Gly) | |
9 | g.36246216T>G | CA373418722 | CLTA,GNE | c.524A>C (p.Asp175Ala) c.254A>C (p.Asp85Ala) c.431A>C (p.Asp144Ala) c.486-16982T>G (n.486-16982T>G) c.416A>C (p.Asp139Ala) | |
9 | g.36246217C>A | CA373418724 | CLTA,GNE | c.523G>T (p.Asp175Tyr) c.253G>T (p.Asp85Tyr) c.430G>T (p.Asp144Tyr) c.486-16981C>A (n.486-16981C>A) c.415G>T (p.Asp139Tyr) | gnomAD v4 |
9 | g.36246217C>G | CA373418726 | CLTA,GNE | c.523G>C (p.Asp175His) c.253G>C (p.Asp85His) c.430G>C (p.Asp144His) c.486-16981C>G (n.486-16981C>G) c.415G>C (p.Asp139His) | gnomAD v4 |
9 | g.36246217C>T | CA373418727 | CLTA,GNE | c.523G>A (p.Asp175Asn) c.253G>A (p.Asp85Asn) c.430G>A (p.Asp144Asn) c.486-16981C>T (n.486-16981C>T) c.415G>A (p.Asp139Asn) | |
9 | g.36246218A= | CA1846375436 | CLTA,GNE | c.522T= (p.Asp174=) c.252T= (p.Asp84=) c.429T= (p.Asp143=) c.486-16980A= (n.486-16980A=) c.414T= (p.Asp138=) | |
9 | g.36246218A>C | CA373418730 | CLTA,GNE | c.522T>G (p.Asp174Glu) c.252T>G (p.Asp84Glu) c.429T>G (p.Asp143Glu) c.486-16980A>C (n.486-16980A>C) c.414T>G (p.Asp138Glu) | |
9 | g.36246218A>G | CA464619996 | CLTA,GNE | c.522T>C (p.Asp174=) c.252T>C (p.Asp84=) c.429T>C (p.Asp143=) c.486-16980A>G (n.486-16980A>G) c.414T>C (p.Asp138=) | ClinVar dbSNP |
9 | g.36246218A>T | CA373418732 | CLTA,GNE | c.522T>A (p.Asp174Glu) c.252T>A (p.Asp84Glu) c.429T>A (p.Asp143Glu) c.486-16980A>T (n.486-16980A>T) c.414T>A (p.Asp138Glu) | gnomAD v4 |
9 | g.36246219T>A | CA373418734 | CLTA,GNE | c.521A>T (p.Asp174Val) c.251A>T (p.Asp84Val) c.428A>T (p.Asp143Val) c.486-16979T>A (n.486-16979T>A) c.413A>T (p.Asp138Val) | |
9 | g.36246219T>C | CA373418738 | CLTA,GNE | c.521A>G (p.Asp174Gly) c.251A>G (p.Asp84Gly) c.428A>G (p.Asp143Gly) c.486-16979T>C (n.486-16979T>C) c.413A>G (p.Asp138Gly) | ClinVar gnomAD v4 COSMIC COSMIC COSMIC |
9 | g.36246219T>G | CA373418736 | CLTA,GNE | c.521A>C (p.Asp174Ala) c.251A>C (p.Asp84Ala) c.428A>C (p.Asp143Ala) c.486-16979T>G (n.486-16979T>G) c.413A>C (p.Asp138Ala) | |
9 | g.36246220C>A | CA373418740 | CLTA,GNE | c.520G>T (p.Asp174Tyr) c.250G>T (p.Asp84Tyr) c.427G>T (p.Asp143Tyr) c.486-16978C>A (n.486-16978C>A) c.412G>T (p.Asp138Tyr) | |
9 | g.36246220C>G | CA373418742 | CLTA,GNE | c.520G>C (p.Asp174His) c.250G>C (p.Asp84His) c.427G>C (p.Asp143His) c.486-16978C>G (n.486-16978C>G) c.412G>C (p.Asp138His) | |
9 | g.36246220C>T | CA373418744 | CLTA,GNE | c.520G>A (p.Asp174Asn) c.250G>A (p.Asp84Asn) c.427G>A (p.Asp143Asn) c.486-16978C>T (n.486-16978C>T) c.412G>A (p.Asp138Asn) | |
9 | g.36246221A>C | CA373418746 | CLTA,GNE | c.519T>G (p.Ile173Met) c.249T>G (p.Ile83Met) c.426T>G (p.Ile142Met) c.486-16977A>C (n.486-16977A>C) c.411T>G (p.Ile137Met) | |
9 | g.36246221A>G | CA464620002 | CLTA,GNE | c.519T>C (p.Ile173=) c.249T>C (p.Ile83=) c.426T>C (p.Ile142=) c.486-16977A>G (n.486-16977A>G) c.411T>C (p.Ile137=) | |
9 | g.36246221A>T | CA464620000 | CLTA,GNE | c.519T>A (p.Ile173=) c.249T>A (p.Ile83=) c.426T>A (p.Ile142=) c.486-16977A>T (n.486-16977A>T) c.411T>A (p.Ile137=) | |
9 | g.36246222A= | CA1846375443 | CLTA,GNE | c.518T= (p.Ile173=) c.248T= (p.Ile83=) c.425T= (p.Ile142=) c.486-16976A= (n.486-16976A=) c.410T= (p.Ile137=) | |
9 | g.36246222A>C | CA373418749 | CLTA,GNE | c.518T>G (p.Ile173Ser) c.248T>G (p.Ile83Ser) c.425T>G (p.Ile142Ser) c.486-16976A>C (n.486-16976A>C) c.410T>G (p.Ile137Ser) | |
9 | g.36246222A>G | CA373418750 | CLTA,GNE | c.518T>C (p.Ile173Thr) c.248T>C (p.Ile83Thr) c.425T>C (p.Ile142Thr) c.486-16976A>G (n.486-16976A>G) c.410T>C (p.Ile137Thr) | ClinVar dbSNP gnomAD v4 |
9 | g.36246222A>T | CA373418752 | CLTA,GNE | c.518T>A (p.Ile173Asn) c.248T>A (p.Ile83Asn) c.425T>A (p.Ile142Asn) c.486-16976A>T (n.486-16976A>T) c.410T>A (p.Ile137Asn) | |
9 | g.36246223T>A | CA373418755 | CLTA,GNE | c.517A>T (p.Ile173Phe) c.247A>T (p.Ile83Phe) c.424A>T (p.Ile142Phe) c.486-16975T>A (n.486-16975T>A) c.409A>T (p.Ile137Phe) | |
9 | g.36246223T>C | CA373418756 | CLTA,GNE | c.517A>G (p.Ile173Val) c.247A>G (p.Ile83Val) c.424A>G (p.Ile142Val) c.486-16975T>C (n.486-16975T>C) c.409A>G (p.Ile137Val) | |
9 | g.36246223T>G | CA373418758 | CLTA,GNE | c.517A>C (p.Ile173Leu) c.247A>C (p.Ile83Leu) c.424A>C (p.Ile142Leu) c.486-16975T>G (n.486-16975T>G) c.409A>C (p.Ile137Leu) | |
9 | g.36246224G>A | CA464620007 | CLTA,GNE | c.516C>T (p.Thr172=) c.246C>T (p.Thr82=) c.423C>T (p.Thr141=) c.486-16974G>A (n.486-16974G>A) c.408C>T (p.Thr136=) | dbSNP gnomAD v2 gnomAD v4 |
9 | g.36246224G>C | CA464620009 | CLTA,GNE | c.516C>G (p.Thr172=) c.246C>G (p.Thr82=) c.423C>G (p.Thr141=) c.486-16974G>C (n.486-16974G>C) c.408C>G (p.Thr136=) | |
9 | g.36246224G= | CA1846375446 | CLTA,GNE | c.516C= (p.Thr172=) c.246C= (p.Thr82=) c.423C= (p.Thr141=) c.486-16974G= (n.486-16974G=) c.408C= (p.Thr136=) | |
9 | g.36246224G>T | CA464620008 | CLTA,GNE | c.516C>A (p.Thr172=) c.246C>A (p.Thr82=) c.423C>A (p.Thr141=) c.486-16974G>T (n.486-16974G>T) c.408C>A (p.Thr136=) | |
9 | g.36246225G>A | CA373418759 | CLTA,GNE | c.515C>T (p.Thr172Ile) c.245C>T (p.Thr82Ile) c.422C>T (p.Thr141Ile) c.486-16973G>A (n.486-16973G>A) c.407C>T (p.Thr136Ile) | |
9 | g.36246225G>C | CA373418761 | CLTA,GNE | c.515C>G (p.Thr172Ser) c.245C>G (p.Thr82Ser) c.422C>G (p.Thr141Ser) c.486-16973G>C (n.486-16973G>C) c.407C>G (p.Thr136Ser) | |
9 | g.36246225G>T | CA373418763 | CLTA,GNE | c.515C>A (p.Thr172Asn) c.245C>A (p.Thr82Asn) c.422C>A (p.Thr141Asn) c.486-16973G>T (n.486-16973G>T) c.407C>A (p.Thr136Asn) | |
9 | g.36246226T>A | CA373418776 | CLTA,GNE | c.514A>T (p.Thr172Ser) c.244A>T (p.Thr82Ser) c.421A>T (p.Thr141Ser) c.486-16972T>A (n.486-16972T>A) c.406A>T (p.Thr136Ser) | |
9 | g.36246226T>C | CA373418766 | CLTA,GNE | c.514A>G (p.Thr172Ala) c.244A>G (p.Thr82Ala) c.421A>G (p.Thr141Ala) c.486-16972T>C (n.486-16972T>C) c.406A>G (p.Thr136Ala) | |
9 | g.36246226T>G | CA373418768 | CLTA,GNE | c.514A>C (p.Thr172Pro) c.244A>C (p.Thr82Pro) c.421A>C (p.Thr141Pro) c.486-16972T>G (n.486-16972T>G) c.406A>C (p.Thr136Pro) | |
9 | g.36246227C>A | CA464620012 | CLTA,GNE | c.513G>T (p.Gly171=) c.243G>T (p.Gly81=) c.420G>T (p.Gly140=) c.486-16971C>A (n.486-16971C>A) c.405G>T (p.Gly135=) | |
9 | g.36246227C>G | CA464620013 | CLTA,GNE | c.513G>C (p.Gly171=) c.243G>C (p.Gly81=) c.420G>C (p.Gly140=) c.486-16971C>G (n.486-16971C>G) c.405G>C (p.Gly135=) | |
9 | g.36246227C>T | CA464620014 | CLTA,GNE | c.513G>A (p.Gly171=) c.243G>A (p.Gly81=) c.420G>A (p.Gly140=) c.486-16971C>T (n.486-16971C>T) c.405G>A (p.Gly135=) | ClinVar dbSNP |
9 | g.36246228C>A | CA373418780 | CLTA,GNE | c.512G>T (p.Gly171Val) c.242G>T (p.Gly81Val) c.419G>T (p.Gly140Val) c.486-16970C>A (n.486-16970C>A) c.404G>T (p.Gly135Val) | |
9 | g.36246228C>G | CA373418783 | CLTA,GNE | c.512G>C (p.Gly171Ala) c.242G>C (p.Gly81Ala) c.419G>C (p.Gly140Ala) c.486-16970C>G (n.486-16970C>G) c.404G>C (p.Gly135Ala) | |
9 | g.36246228C>T | CA373418786 | CLTA,GNE | c.512G>A (p.Gly171Glu) c.242G>A (p.Gly81Glu) c.419G>A (p.Gly140Glu) c.486-16970C>T (n.486-16970C>T) c.404G>A (p.Gly135Glu) | gnomAD v4 |
9 | g.36246229C>A | CA373418788 | CLTA,GNE | c.511G>T (p.Gly171Trp) c.241G>T (p.Gly81Trp) c.418G>T (p.Gly140Trp) c.486-16969C>A (n.486-16969C>A) c.403G>T (p.Gly135Trp) | |
9 | g.36246229C>G | CA373418791 | CLTA,GNE | c.511G>C (p.Gly171Arg) c.241G>C (p.Gly81Arg) c.418G>C (p.Gly140Arg) c.486-16969C>G (n.486-16969C>G) c.403G>C (p.Gly135Arg) | |
9 | g.36246229C>T | CA373418793 | CLTA,GNE | c.511G>A (p.Gly171Arg) c.241G>A (p.Gly81Arg) c.418G>A (p.Gly140Arg) c.486-16969C>T (n.486-16969C>T) c.403G>A (p.Gly135Arg) | |
9 | g.36246230A= | CA1846375452 | CLTA,GNE | c.510T= (p.Ser170=) c.240T= (p.Ser80=) c.417T= (p.Ser139=) c.486-16968A= (n.486-16968A=) c.402T= (p.Ser134=) | |
9 | g.36246230A>C | CA373418797 | CLTA,GNE | c.510T>G (p.Ser170Arg) c.240T>G (p.Ser80Arg) c.417T>G (p.Ser139Arg) c.486-16968A>C (n.486-16968A>C) c.402T>G (p.Ser134Arg) | |
9 | g.36246230A>G | CA464620017 | CLTA,GNE | c.510T>C (p.Ser170=) c.240T>C (p.Ser80=) c.417T>C (p.Ser139=) c.486-16968A>G (n.486-16968A>G) c.402T>C (p.Ser134=) | ClinVar dbSNP gnomAD v4 |
9 | g.36246230A>T | CA373418800 | CLTA,GNE | c.510T>A (p.Ser170Arg) c.240T>A (p.Ser80Arg) c.417T>A (p.Ser139Arg) c.486-16968A>T (n.486-16968A>T) c.402T>A (p.Ser134Arg) | |
9 | g.36246231C>A | CA373418804 | CLTA,GNE | c.509G>T (p.Ser170Ile) c.239G>T (p.Ser80Ile) c.416G>T (p.Ser139Ile) c.486-16967C>A (n.486-16967C>A) c.401G>T (p.Ser134Ile) | |
9 | g.36246231C>G | CA373418807 | CLTA,GNE | c.509G>C (p.Ser170Thr) c.239G>C (p.Ser80Thr) c.416G>C (p.Ser139Thr) c.486-16967C>G (n.486-16967C>G) c.401G>C (p.Ser134Thr) | |
9 | g.36246231C>T | CA373418811 | CLTA,GNE | c.509G>A (p.Ser170Asn) c.239G>A (p.Ser80Asn) c.416G>A (p.Ser139Asn) c.486-16967C>T (n.486-16967C>T) c.401G>A (p.Ser134Asn) | gnomAD v4 |